Interface for two-part wearable patient monitoring device

ABSTRACT

A two part patient monitoring device includes an activator module and a sensor device. The activator module includes a non-galvanic data port that creates a communication path with a non-galvanic data port on the sensor device. The activator module includes power contact pads that are each at least partially surrounded by a bias ring. A bias voltage is applied to the bias rings and a processor or circuit in the activator module monitors the voltage on the bias ring to detect a leakage current. The sensor module includes power contact pins that engage the power contact pads to transfer power from the activator module to the sensor device. Each of the contact pins are surrounded by a seal member such that the connection between the power contact pins and the power contact pads is protected from debris and/or moisture.

BACKGROUND

The present disclosure relates generally to medical devices and, morespecifically, to medical monitoring devices for monitoring a patient'sphysiology and health status.

In the field of medicine, physicians often desire to monitor multiplephysiological characteristics of their patients. Oftentimes, patientmonitoring involves the use of several separate monitoring devicessimultaneously, such as a pulse oximeter, a blood pressure monitor, aheart monitor, a temperature monitor, etc. Several separate patientmonitoring devices are often connected to a patient, tethering thepatient to multiple bulky bedside devices via physical wiring or cables.Multi-parameter monitors are also available where different sensor setsmay be connected to a single monitor. However, such multi-parametersystems may be even more restrictive than separate monitoring devicesbecause they require all of the sensors attached to a patient to bephysically attached to the monitor, resulting in multiple wires runningacross the patient's body. Thus, currently available patient monitoringdevices often inhibit patient movement, requiring a patient to stay inone location or to transport a large monitor with them when they movefrom one place to another. Further, currently available monitoringdevices are often power intensive and either require being plugged in toa wall outlet or require replacing and recharging the device batteryevery few hours.

SUMMARY

The present disclosure relates to a two part patient monitoring devicethat includes an activator module having at least one power contact pad,a non-galvanic data port and an internal battery. The monitoring devicefurther includes a sensor device that physically connects to theactivator module such that power and data can be transferred therebetween. The sensor device includes at least one sensor, at least onepower contact pin and a second non-galvanic data port. When the sensordevice is connected to the activator module, the power contact pinengages the power contact pad to transfer power between the components.At the same time, the non-galvanic data ports allow data to betransferred between the components without a galvanic connection.

In one embodiment of the disclosure, a seal member surrounds theconnection between the power contact pad and the power contact pin torestrict access to the power connection. In another contemplatedembodiment, a bias ring at least partially surrounds the power contactpad. The bias ring receives a bias voltage and the bias voltage ismonitored by a processor contained in the activator module. Bymonitoring the bias voltage, the processor is able to detect a leakagecurrent at the power connection between the activator module and thesensor device.

In another embodiment of a wireless patient monitor comprises anactivator module having a connection port that connects with any one ofmultiple sensor devices, a battery, and a radio transmitter wirelesslyconnected to a host device. The activator module connects to any one ofmultiple sensor devices via the connection port to provide power fromthe battery to the sensor device and to receive digital physiologicaldata from the sensor device. The radio transmitter transmits the digitalphysiological data received from the sensor device to a host device.

Another embodiment of a patient monitoring system comprises a firstsensor device having a first set of one or more detectors to collect afirst physiological information from a patient, a firstanalog-to-digital converter to convert the first physiologicalinformation to a first digital physiological data, and a first connectorconfigured to transmit the first digital physiological data and toreceive power to power the first sensor device. A second sensor devicehas a second set of one or more detectors to collect secondphysiological information from the patient, a second analog-to-digitalconverter to convert the second physiological information to a seconddigital physiological data, and a second connector configured totransmit the second digital physiological data and to receive power topower the second sensor device. The system further includes an activatormodule capable of alternately connecting with the first sensor deviceand the second sensor device. The activator has a battery, a connectionport configured to connect with the first connector and the secondconnector to provide power from the battery to the first sensor deviceand the second sensor device and to receive digital physiological datafrom the first sensor device and the second sensor device, and a radiotransmitter configured to transmit the first digital physiological dataand the second digital physiological data to a host device.

BRIEF DESCRIPTION OF THE DRAWINGS

The drawings illustrate the best mode presently contemplated of carryingout the disclosure. In the drawings:

FIG. 1 is a block diagram of one embodiment of a wireless patientmonitoring system including a sensor device, a generic activator device,and a host device;

FIG. 2 depicts one embodiment of a wireless patient monitor including afirst sensor device, a second sensor device, and a generic activatormodule;

FIG. 3 depicts another embodiment of a wireless patient monitoringsystem configured to monitor a patient;

FIG. 4 depicts another embodiment of a wireless monitor including an ECGsensor device and a generic activator module;

FIG. 5 depicts another embodiment of a wireless monitor including apulse oximeter sensor device and a generic activator module;

FIG. 6 depicts another embodiment of a wireless monitor including ablood pressure sensor device and a generic activator module;

FIG. 7 depicts another embodiment of a wireless monitor including atemperature sensor device and a generic activator module;

FIG. 8 is a front perspective view of one embodiment of the activatormodule;

FIG. 9 is a bottom view of the activator module of FIG. 8;

FIG. 10 is a front perspective view of one embodiment of the sensordevice;

FIG. 11 is a top view of the sensor device shown in FIG. 10;

FIG. 12A is a first embodiment of the contact pad and bias ring;

FIG. 12B is a second embodiment of the contact pad and bias ring;

FIG. 13 is a partial section view showing the contact pin mounted withinthe sensor device; and

FIG. 14 is a circuit schematic showing the monitoring of the biasvoltage applied to the bias rings at least partially surrounding thefirst and second contact pads.

DETAILED DESCRIPTION OF THE INVENTION

FIG. 1 depicts one embodiment of a wireless patient monitoring system 1including a sensor device 2, a generic activator module 3 and a hostdevice 4. FIG. 2 depicts one embodiment of a wireless patient monitoringsystem demonstrating the interaction between one or more sensor devicesand the generic activator module 3. The generic activator module 3 isconnectable with any one of several different types of sensor devices 2to provide power to the sensor device 2 and to transmit the digitalphysiological data produced by the sensor device 2 to a host device 4. Amonitoring system, such as that shown in FIG. 2, may further include anynumber of generic activator modules 3 that are interchangeable with oneanother and are each configured to pair with any of the available typesof sensor devices. The generic activator modules 3 may be rechargeable,such as by containing rechargeable batteries, and may be interchanged inorder to maintain power to any sensor device 2.

For example, the generic activator module 3 demonstrated in FIG. 2 isconnectable to any one of a number of different sensor devices 2 such asthe first sensor device 47 and the second sensor device 50. The firstsensor device 47 has a first set of patient sensors 49, and the secondsensor device 50 has a second set of patient sensors 52. The firstsensor device 47 and the second sensor device 50 may be any devices forsensing patient physiological data. For example, the first sensor device47 may be an ECG sensor device wherein the first patient sensors 49 areECG leads, and the second sensor device 50 may be an EEG sensor devicewherein the second patient sensors 52 are EEG leads. The genericactivator module 3 of FIG. 2 may be inserted into or otherwise connectedwith either of the first sensor device 47 or the second sensor device 50to activate that device 47 or 50 and transmit the data collected by thatdevice to the host device. Such connection is made by positioninggeneric activator module 3 so that the universal connection port 16 ofthe generic activator module 3 is in contact with the connector 48 ofthe first sensor device 47 or the connector 51 of the second sensordevice 50. It should be understood that contact between the genericactivator module 3 and the first or second sensor devices 47, 50 may bean electrical contact or any other connection that allows communicationand power transfer. In alternative embodiments, the connection may bethrough means not requiring galvanic contact between the genericactivator module 3 and the first or second sensor devices 47, 50. Forexample, the generic activator module 3 may be connected to the first orsecond sensor devices 47, 50 via an optical data transfer and acapacitive power transfer. Additionally, the generic activator module 3may be configured to process the physiological data from the varioussensor devices, such as the EEG data or ECG data in the present example,and/or to display physiological information about the patient derivedfrom the physiological data.

Returning to FIG. 1, the depicted embodiment has a sensor device 2 withone or more patient sensors or detectors 8 connected to a processor 10.The one or more patient detectors 8 may include any sensors, leads, orother devices available in the art for sensing or detectingphysiological information from a patient, which may include but are notlimited to electrodes, lead wires, or available physiologicalmeasurement devices such as blood pressure cuffs, pulse oximetrysensors, temperature sensors, etc. The physiological signals recorded bythe patient detectors 8 are digitized by analog-to-digital converter(A/D converter) 9. The A/D converter 9 may be any device or logic setcapable of digitizing analog physiological signals. For example, the A/Dconverter 9 may be an Analog Front End (AFE). Processor 10 receives thedigital physiological data from the A/D converter 9 and may transmit theprocessed data and the raw digitized physiological data to the genericactivator module 3 via the connector 14.

The processor 10 may be configured to perform various functionsdepending on the type of sensor device 2 detected. For example, if thesensor device 2 is a noninvasive blood pressure (NIBP) monitor then theprocessor may be configured to process the physiological data detectedby the sensors in a blood pressure cuff to calculate systolic, diastolicand mean blood pressure values. Likewise, the processor 10 may also beconfigured to determine a heart rate when the generic activator module 3is connected to an ECG sensor device. Likewise, the processor 10 may beconfigured to determine a blood oxygenation value for the patient whenthe generic activator module 3 is connected to a sensor device 2 that isa pulse oximeter sensor device. Likewise, the processor 10 may beconfigured to also detect when it is connected to anelectroencephalograph (EEG) sensor device and then determine a depth ofanesthesia measurement value, such as an entropy value or a sedationresponsiveness index value. In an embodiment where the sensor device 2is a thermometer or temperature sensor device, the processor 10 may beconfigured to determine a temperature for the patient, such as a meantemperature. Alternatively or additionally, the processor 26 of thegeneric activator module 3 may be configured to process the digitalphysiological data from the sensor device 2 to calculate any or all ofthose aforementioned values. It should be understood that the device andsystem of the present disclosure is not limited to the examplesprovided, but may be configured and employed to monitor any clinicalparameter. The examples provided herein are for the purpose ofdemonstrating the invention and should not be considered limiting.

In another alternative embodiment, the sensor device 2 may not containany processor. In such an embodiment, the digitized physiological datawould be sent from the A/D converter 9 of the sensor device 2 to thegeneric activator module 3. Accordingly, the generic activator module 3may be configured to receive digitized raw data or digitized filtereddata from various types of sensor devices 2, which is the physiologicaldata detected by the patient detectors 8 of the various sensor devicesthat has been digitized by the A/D converter 9.

The processor 10 and the A/D converter 9 receive power from the powersupply 12. The power supply 12 may be a simple conductor that conductspower received from the generic activator module 3 via the connector 14.Alternatively, the power supply 12 may include a battery that storesenergy received from the generic activator module 3 and distributes thatpower to the various powered elements of the sensor device 2. Moreover,the power supply 12 may further include power management capabilities.This may be the case in embodiments where the sensor device 2 containsmore demanding electromechanical aspects, such as a noninvasive bloodpressure monitor. In other embodiments where the sensor device 2 hasonly simple components, such as an embodiment only having patientsensors 8 and an analog to digital converter 9, the power managementcapabilities may not be necessary and may be excluded from the sensordevice 2.

The sensor device 2 has a connector 14 that is configured to connectwith the universal connection port 16 on the generic activator module 3.The connector 14 and the universal connection port 16 may be configuredin any manner known in the art for performing the functions describedherein. The purpose of the interface is to transfer power to the sensordevice 2 and data to and from the sensor device 2. Examples of methodsfor transferring power though the interface 14, 16 are through galvanicconnectors, through inductive or capacitive coupling. Examples ofmethods for transferring data through the interface 14, 16 are throughgalvanic connectors or using optical data transfer. In one embodiment,the connector 14 and the universal connection port 16 may each be auniversal asynchronous receiver/transmitter (UART), and thus may includean integrated circuit to translate data between parallel and serialforms. The universal connection port 16 and the connection port 14 mayalternatively be I²C or Serial Peripheral Interface (SPI). The datacommunication between the sensor device 2 and the activator module 3 mayalternatively be implemented using RF communication such as Bluetooth,near field communication (NFC), ANT or any other protocol suitable forshort range communication. Due to the close proximity of the sensordevice 2 and the activator module 3, the RF power required and theantennae can be optimized to provide very local RF communication.

In any embodiment, the universal connection port 16 is configured toreceive and connect with the connectors 14 of various types of sensordevices 2. For example, the connector 14 may be configured identicallyfor all types of sensor devices 2. In other embodiments, the connector14 may be configured differently for various types of sensor devices 2.For example, the connector may have more or less connection points fortransmitting digitized physiological data and power depending on thetype of sensor device 2 and how many data channels are collected. Theconnection points may be electrical contact points, aligned inductivecoils, aligned optical components, or any connects capable oftransferring data and power between the generic activator module 3 and asensor device. As another example, the connector 14 may provide aconnection point to an identification chip or element 13 in a sensordevice 2 to provide an identification pin for the sensor device 2 to thegeneric activator module 3. Alternatively, in other sensor devices 2 anidentification pin for the sensor device 2 to the generic activatormodule 3 may be provided by a processor 10. The universal connectionport 16 may be configured to connect with each such connector of varioussensor devices.

When the connector 14 of the sensor device 2 is connected the genericactivator module 3, power is provided from the generic activator module3 to the sensor device 2, and digital physiological data is providedfrom the sensor device 2 to the generic activator module 3.Additionally, the sensor device 2 may identify itself to the genericactivator module 3 through the connector 14 in communication with theuniversal connection port 16. A sensor device 2 may have anidentification chip or element 13 which provides an identification pinfor that sensor device 2. In the embodiment of FIG. 1, theidentification device 13 of the sensor device 2 is in communication withthe identification receiver 18 of the generic activator module 3. Theidentification receiver 18 then communicates the identification pin tothe processor 26 of the generic activator module 3 such that the genericactivator module 3 can identify the sensor device 2 to which it isconnected. In another embodiment, the processor 10 of the sensor device2 may directly provide an identification pin through the connector 14and the universal port 16 to the processor 26 of the generic activatormodule 3. In such an embodiment, a sensor device 2 may not contain anyidentification device 13. However, in embodiments where the sensordevice 2 does not have a processor or where the processor of a sensordevice 2 does not provide an identification pin, the identificationdevice 13 may be employed.

In the embodiment of FIG. 1, the generic activator module 3 has aprocessor 26 that receives digital physiological data transmitted fromthe sensor device 2. The processor 26 may be configured to process thedigital physiological data prior to transmitting the data to the hostdevice 4 or displaying the physiological data on the user interfacedisplay 24. In other embodiments, the processor 26 of the genericactivator module 3 may not process the digital physiological data atall, as generic activator module 3 may receive digital physiologicaldata from a sensor device 2 and relay that data to a host device 4 via awireless connection to the host device. As described with respect toexemplary embodiments herein, the processor 26 may be configured todetect the type of sensor device 2 to which the generic activator module3 is connected and to conduct various levels of data processingdepending on the configuration of the generic activator module 3 anddepending on the sensor device 2 to which the generic activator module 3happens to be connected.

The processor 26 may also control the user interface display 24 todisplay physiological information about the patient. The displayedphysiological information may be calculated by the processor 26 based onthe digital physiological data received from the sensor device 2 or bythe processor 10 in the sensor device. For example, if the sensor device2 is an ECG sensor device 42 (FIG. 3), the processor 26 may processdigital ECG data received from the ECG sensor device to calculate aheart rate, and then may display the heart rate on the user interfacedisplay 24. In an alternative embodiment, the ECG sensor device 42 maycontain a processor 10 that calculates the heart rate on the digital ECGdata. In such an embodiment, the processor 26 of the generic activatormodule may simply operate to display the heart rate calculated at theECG sensor device 42 on the UI display 24.

The processor 26 may operate radio frequency antenna/transmitter 28 totransmit data to a host device 4, where the data may be furtherprocessed and/or stored. The radio frequency antenna/transmitter 28 ofthe generic activator module 3 and the RF antenna/transmitter 30 of thehost device 4 may be any devices known in the art for wirelesslytransmitting data between two points. In one embodiment, the RFantenna/transmitters 28 and 30 may be body area network (BAN) devices,such as medical body area network (MBAN) devices, that operate as awireless network of wearable or portable computing devices. In such anembodiment, one or more generic activator modules 3 which may beconnected to various sensor devices 2 attached to the patient may be incommunication with a host device 4 positioned in proximity of thepatient. Other examples of radio protocols that could be used for thispurpose are Bluetooth, Bluetooth Low Energy (BLE), ANT and ZigBee.

For example, turning to FIG. 3, a patient 56 may be monitored by two ormore sensor devices 2, such as a noninvasive blood pressure sensordevice 65 and a pulse oximeter sensor device 67. Each of the sensordevices 65 and 67 may be engaged with a generic activator module 3 toactivate and power the sensor devices 65 and 67 and transmit the datacollected by each of the sensor devices 65 and 67 to a host device 4. Inan embodiment where the host device 4 is a part of a BAN, the hostdevice 4 would be in proximity to the patient 56, such as attached tothe patient's body, placed on or near the patient's bed, or positionedwithin range of the patient such as in the same room as the patient.

Any host device 4 may have a user interface 36 which may display datafrom the various sensor devices 65 and 67 on the same BAN for thepatient 56. The host device 4 may further transmit the physiologicaldata for the patient gathered by the sensor devices 65 and 67 to acentral monitoring station 73 and/or to a central storage location 75.The central monitoring station 73 may provide a central location forattending clinicians to monitor patient status and/or receive alarmnotifications. The central monitoring station 73 may be a local networkhaving servers housed within a medical facility, or it may be acloud-based system hosted by a cloud computing provider. The centralstorage 75 may be a central storage location for patient information tobe stored long term, such as information that may become part of apatient's medical record and/or may be accessible by an attendingclinician from any remote location.

In another embodiment, the host device 4 may be a remote device, such ascentral hub for a network of many monitoring devices within a healthcarefacility or a subset of a healthcare facility. In such an embodiment,the RF receiver/transmitter 28 of the generic activator module and theRF receiver/transmitter 30 of the host device may operate on alonger-range wireless network, such as a network operating on thewireless medical telemetry service (WMTS) spectrum or on aWiFi-compliant wireless local area network (WLAN). In such anembodiment, the host device 4 may be receiving digital physiologicaldata from two or more generic activator modules 3 connected to differentpatients within range of the host device 4. For example, a host devicemay be associated with a section of a healthcare facility, such as aunit or a floor, and may receive digital physiological data from all ofthe patients in that area.

The processor 26 may be further configured to operate the power gaugeand protection module 22 which is connected to the battery 20. Thereby,the processor 26 and the power gauge and protection module 22 mayregulate the power distribution within the generic activator module 3and the sensor device 2. For example, the power from the battery 20 maybe distributed to power the processor 26, the UI display 24 and the RFantenna/transmitter 28 in the generic activator module. The battery 20may be any battery capable of providing sufficient power, and ispreferably a rechargeable battery. Further, when the generic activatormodule 3 is connected to a sensor device 2, power is further distributedfrom the battery 20 through the power gauge and protection module 22 tothe sensor device 2 through the universal connection port 16 and theconnector 14. As described above, the sensor device 2 may have a powersupply module 12 that distributes power within the sensor device 2.Alternatively, the power gauge and protection module 22 may distributepower directly to devices within the sensor device 2, such as to the A/Dconverter 9, processor 10, and/or identification device 13.

The host device 4 has receiver/transmitter 30 which is in communicationwith the RF receiver/transmitter 28 and the generic activator module 3.The host device may further comprise a processor 32, a user interface36, and digital storage 34. The processor 32 may further process digitalphysiological data received from one or more generic activator modules 3in communication with the host device 4. The host device may furtherdisplay the patient's physiological information on the user interface36. The user interface 36 may be utilized by a clinician to view detailsof the digital physiological data collected by the sensor devices 2. Theuser interface 36 of the host device 4 may be used by a clinician toview aspects of the digital physiological data for the patient that arenot viewable on the display of the generic activator module 3. Forexample, in an embodiment where a sensor device 2 is an ECG sensordevice 42, a clinician may not be able to review ECG waveforms recordedby the ECG sensor device 42 on the user interface 36 of the host device4 because, in some embodiments, the user interface display 24 of thegeneric activator module 3 may be too small to display full waveforms,such as ECG waveforms.

The host device 4 may also have a digital storage device 34 for storingthe physiological data collected by the various sensor devices 2 incommunication with the host device 4 through various generic activatormodules 3. The storage location 34 may also store processedphysiological data created by the processor 32 of the host device, theprocessor 26 of the generic activator module 3, and/or the processor 10of the sensor device 2.

The sensor devices 2 may be attached to the patient by variousmechanisms so that the wireless patient monitoring devices can be worn,or maintained, on or near the patient and the patient can remain mobileand not get tangled, disconnected, or loosing monitoring. For example,as shown in FIG. 3, the noninvasive blood pressure sensor device 65 maybe attached to the blood pressure cuff 66 which may be worn by thepatient. Likewise, the pulse oximeter sensor device 67 may be attachedto wristband 69 which may be worn by the patient. In other embodiments,various sensor devices 2 may be attached to the patient by various meanswhich are proximate to the area where the patient detectors 8 areattached to the patient. For example, an ECG sensor device 42 (FIG. 4)may be connected to the patient via a chest strap or a waist strap. Inanother embodiment, an EEG sensor device may be attached to a patient bya headband, neckband, chest band, or armband, or may be attacheddirectly to an ECG electrode or a separate accessory adhered to the skinof the patient. The generic activator module 3 would then connect to andbe worn with each sensor device 2 wherever that sensor device iscontained on the patient.

Exemplary displays 24 for generic activator modules 3 are provided inFIGS. 4-7. FIG. 4 depicts an ECG sensor device 42 connected to a genericactivator module 3. The ECG sensor device 42 has ECG detectors 43 thatcollect ECG data from a patient. It should be understood that the ECGdetectors 42 may be any sensors, leads, or other devices capable ofdetecting patient cardiac signals. In the embodiment of FIG. 4, thedisplay 24 of the generic activator module 3 displays the letters “ECG”on the connected device indicator 79 to signify that the genericactivator module 3 is connected to an ECG sensor device 42.

The display 24 in FIG. 4 also displays a heart rate in beats per minute(BPM), which may be calculated by a processor in the generic activatormodule 3 or in the sensor device 2 based on the physiological datacollected by the detectors 43. The display 24 may also provide awireless connection status indicator 77 to indicate the status of theconnection between the generic activator module 3 and the host device 4.The wireless connection status indicator 77 in FIG. 4 is a series archedlines that light up to show the wireless connection strength between thegeneric activator module 3 and the host device 4. However, the wirelessconnection status indicator 77 may take on any form capable ofcommunicating the connectivity strength or status between the RFreceiver/transmitter 28 of the generic activator module 3 and the RFreceiver/transmitter 30 of the host device 4. For example, the wirelessconnection status indicator 77 may simply indicate the presence orabsence of a wireless connection between the generic activator module 3and the host device 4. The display 24 may also have a charge statusindicator 78 to indicate the charge level of the battery in the genericactivator module 3. The display 24 may also have an indicator toindicate the pairing status of the sensor (not shown), i.e. if thesensor is currently paired to a host device.

Additionally, the display unit may contain a detector status indicator80 to indicate the status of the detectors 43 and their connectivity tothe patient. In the embodiment shown in FIG. 4, the detector statusindicator 80 is a series of five dots, each representing one of thedetectors 43. The fourth dot is provided with an “x” through it toindicate that the sensor associated with that dot is not properlyconnected to the patient. This may be because the lead and/or the sensorare not properly connected to the patient, or it may be due to a failureof the detector device. In other embodiments, the detector statusindicator 80 may be provided in any manner that would effectivelycommunicate whether the detectors 43 are properly functioning anddetecting physiological information from the patient. For example, thedisplay 24 may provide a “sensor off” notification if a detector 43 isnot properly connected to a patient, or it may provide a “sensorfailure” notification if a detector 43 is not functioning properly.

The display 24 may also provide various other indicators. In otherembodiments, the display 24 may offer a system function indicator toindicate whether the sensor device 2 and/or the generic activator module3 are functioning properly and, if a malfunction occurs, indicate whatthe malfunction or problem is.

FIG. 5 depicts a pulse oximeter sensor device 81 connected to a genericactivator module 3. The pulse oximeter sensor device 81 has a pulseoximeter detector 82 that attaches to a patient, such as the patient'sfinger or ear, to measure blood oxygenation. In the embodiment of FIG.5, the display 24 of the generic activator module 3 provides a connecteddevice indicator 79 displaying “SpO₂” and an SpO₂ percentage valuecalculated based on the measurements taken by the pulse oximeterdetector 82 connected to a patient.

FIG. 6 provides an example embodiment of a noninvasive blood pressure(NIBP) sensor device 85 paired with a generic activator module 3. TheNIBP sensor device 85 has a blood pressure cuff 86 to noninvasivelymeasure a patient's blood pressure. The information gathered by thenoninvasive blood pressure cuff 86 is communicated from the NIBP sensordevice 85 to the generic activator module 3 as described above. Thedisplay 24 of the generic activator module 3 provides a connected deviceindicator 79 displaying “NIBP” to indicate that the generic activatormodule 3 is paired with an NIBP sensor device 85. The display 24 alsodisplays the blood pressure value for the patient as well as thepatient's pulse rate, which are values calculated based on the bloodpressure data measured by the blood pressure cuff 86.

FIG. 7 depicts an embodiment of a temperature sensor device 88 connectedto a generic activator module 3. The temperature sensor device 88 has atemperature detector 89 which is attachable to a patient to measure thepatient's temperature. The temperature detector 89 may be, for example,an adhesive thermometer device that adheres to a patient, such as on apatient's forehead, neck, or armpit, to measure the temperature of thatlocation on the patient or a central temperature sensor, such as acatheter. The display 24 of the generic activator module 3 has aconnected device indicator 79 displaying “temp” to indicate that thegeneric activator module 3 is paired with a temperature sensor device88. Further, the display 24 of FIG. 7 is displaying a temperaturemeasured by the temperature sensor device, which is displayed as 98° F.Likewise, the wireless connection status indicator indicates thewireless connection status of the generic activator module 3 and thecharge status indicator 78 indicates the battery charge of the genericactivator module 3.

Each type of sensor device 2, such as those described herein, may havevarying levels of complexity. For example, the ECG sensor device 42 ofFIG. 4 may contain a processor to process the ECG data collected by thedetectors 43 to determine or calculate information based on the measuredcardiac signals, such as heart rate and/or the presence of abnormalwaveforms. In other embodiments, the ECG sensor device 42 may notcontain any processor 10 and the digitized raw physiological data may besent from the ECG sensor device 42 to the generic activator module 3there to bear with. In such an embodiment, the generic activator module3 may contain a processor that processes the digitized raw ECG datadetected by the ECG sensor device 42. In still other embodiments, thegeneric activator module 3 may not process the digitized raw ECG dataand may simply relay the data to the host device 4 via the RFreceiver/transmitter 28 housed therein.

Certain sensor devices may be larger and more complicated and thus maynecessitate having an internal processor 10 and/or an internal powersupply 12 housed therein. For example, an NIBP sensor device 85 requiresmore significant electromechanical elements to operate the bloodpressure cuff which may require power management to be internal to theNIBP sensor device 85. Thus, it may be preferable to house a processor10 within the NIBP sensor device 85 which can process the physiologicaldata gathered by the blood pressure cuff 86. Conversely, the temperaturesensor device 88 may be a very simple device, and it may be preferableto not include a processor or power management within the temperaturesensor device 88. In one embodiment, the temperature sensor device 88may be a disposable device, and thus for cost reasons, it would bepreferable to limit the amount of elements in the temperature sensordevice 88 to limit the cost of the disposable device.

As discussed previously, FIG. 2 illustrates a first embodiment for thephysical configuration for the activator module 3 and the sensor device2, illustrated by the pair of sensor devices 47, 50 shown in FIG. 2.Although this physical configuration is illustrated as one exemplarilyembodiment, various different physical configurations are contemplatedas being within the scope of the present disclosure.

FIGS. 8 and 9 illustrate a first, alternate embodiment for the physicalconfiguration of the activator module 3 constructed in accordance withthe present disclosure. The activator module 3 shown in FIGS. 8 and 9includes a molded outer housing 90 that includes a front surface 92including the display 24, not shown in FIG. 8 but as illustrated in theembodiments of FIGS. 4-7. The rear surface 94 is designed including areceiving channel 96. The receiving channel 96 is recessed from the rearsurface 94. The recessed receiving channel 96 is sized to receive theconnecting portion 98 of the sensor device 2, which is shown in FIGS. 10and 11. The connecting portion 98 extends from the sensor housing 100and is sized to securely fit within the receiving channel 96. When theconnecting portion 98 is received in the receiving channel 96, thesensor device 2 is able to transmit data to the activator module andreceive power from the activator module as will be described in greaterdetail below.

Referring back to FIG. 8, the outer housing 90 includes a generallyplanar front face 102. A contact face surface 104 is angled relative toboth the front face 102 and the base wall 106 of the receiving channel96. The contact face surface 104 includes both a first contact pad 108and a second contact pad 110. The first and second contact pads 108, 110are internally connected to the battery 20 contained within theactivator module, as shown in FIG. 1. The pair of contact pads 108, 110form part of the generic connection port 16 shown in FIG. 1.

Referring back to FIGS. 8 and 9, in addition to the pair of contact pads108, 110, the activator module 3 includes an optical data port 112 thatis able to both transmit and receive data through an optical datatransmission path. The optical data port 112 is formed within agenerally flat face surface 114 that extends above the base wall 106 ofthe receiving channel 96. The optical data port 112 is sized andpositioned to receive data signals from the sensor device when thesensor device is mated with the activator module 3, as will be describedin detail below.

FIGS. 12A and 12B illustrate two separate embodiments of the first andsecond contact pads 108, 110. In the first embodiment shown in FIG. 12A,the contact pad 108 includes a metallic contact 116 at least partiallysurrounded by a bias ring 118. In the embodiment shown in FIG. 12B, themetallic contact 116 is completely surrounded by the bias ring 118.Although two separate embodiments are shown in FIGS. 12A and 12B, it iscontemplated that either embodiment could be utilized while operatingwithin the scope of the present disclosure.

As illustrated in FIGS. 12A and 12B, each of the metallic contacts 116includes a recessed receptacle 120 that provides a receiving locationfor a mating contact pin of the sensor device as will be described indetail below. The bias ring 118, whether completely surrounding thecontact 116 or only partially surrounding the contact 116, is formedfrom an electrically conductive material. A non-conductive gap 122 isformed between the metallic contact 116 and the bias ring 118 torestrict the flow of current between the contact 116 and the bias ring118. However, if a conductive or partially conductive material or liquidis located within the gap 122, current will be able to flow from thebias ring 118 to the contact 116, as will be described in greater detailbelow.

Referring now to FIGS. 10 and 11, the sensor device 2 of the presentdisclosure is designed to mate with the activator module 3 such thatdata and power can be transmitted between the two devices. In theembodiment illustrated, the connecting portion 98 includes an opticaldata port 124 that is formed in the generally flat face surface 126. Ascan be understood in the comparison between FIGS. 9 and 10, the opticaldata port 112 formed on the activator module 3 and the optical data port124 formed on the sensor device 2 are designed to be physically alignedwith each other such that an optical data path can be formed to transmitdata to and from the sensor device 2 through the mating optical dataports.

As illustrated in FIGS. 10 and 11, the sensor device 2 includes a firstcontact pin 128 and a second contact pin 130. Both the first and secondcontact pins 128, 130 are located within and as part of a contact facesurface 132 that is inclined relative to the generally planar facesurface 126. A pair of side walls 134 define and support the contactface surface 132 relative to the planar face surface 126.

Referring now to FIG. 13, each of the first and second contact pins 128is formed from a metallic member having a domed outer surface 136. Thecontact pin 128 is connected to a spring arm 138 that exerts anoutwardly directed physical bias force on the contact pin 128 to urgethe contact pin 128 into contact with the corresponding contact pad onthe activator device when the two components are mated. As can beillustrated in FIG. 13, the connecting portion 98 and the housing 100are formed from different types of molded plastic material.Specifically, the majority of the connecting portion 98 is formed from agenerally rigid plastic first material 140 while a second, more flexibleplastic material 142 is used to mount the contact pin 128. The secondmaterial 142 is resilient and flexible compared to the first material140, which allows the contact pin 128 to flex.

The second, flexible plastic material 142 forms a seal 144 thatprotrudes above the mounting surface 146. The mounting surface 146surrounds and supports the contact pin 128. As illustrated, separateseals 144 surround the first contact pin 128 and the second contact pin130. However, it is contemplated that a single, continuous seal could beused that would surround both of the contact pins 128 and 130. As can beunderstood in the comparisons of FIGS. 8 and 10, when the sensor device2 mates with the activator module 3, the seals 144 surrounding each ofthe first and second contact pins 128, 130 engage the generally flatcontact face surface 104 to provide a generally fluid-tight seal thatsurrounds the electrical contact between the first and second contactpins 128, 130 on the sensor device 2 and the first and second contactpads 108, 110 on the activator module 3.

Since the seal 144 surrounds the electrical contact between the contactpins 128, 130 and the contact pads 108, 110, the sealing arrangementlimits the amount of debris, liquid or other elements that can affectthe power transfer from the activator module to the sensor device.

FIG. 14 illustrates control circuitry that is contained within theactivator module 3 to monitor for leakage current that may be generateddue to a fault in the connection between the activator module 3 and thesensor device 2. As illustrated in the circuit diagram of FIG. 14, thefirst contact pad 108 is connected to the positive terminal 150 of thebattery power supply contained within the activator module. The secondcontact pad 110 is connected to ground 151 such that power can betransferred from the activator module to the sensor device when thefirst and second contact pads 108, 110 are positioned in contact withthe first and second contact pins formed as part of the sensor device.As discussed previously, a bias ring 118 surrounds or partiallysurrounds each of the first and second contact pads 108, 110. In theembodiment illustrated, the bias ring 118 surrounding the first contactpad 108 is connected to the current leakage detection pin 152 of theprocessor 26 while the second bias ring 118 surrounding the secondcontact pad 110 is connected to a second current leakage detection pin154. Each of the bias rings 118 is connected to the respective currentleakage pin 152, 154 through a separate current limiting resistor 156.The current limiting resistors are selected having a relatively highresistance to limit the current flowing to the respective pins 152, 154.Although the first and second bias rings 118 are shown and described asbeing connected to pins on the processor 26, it is contemplated that aseparate detection circuit could be used, which would then communicatewith the processor 26.

In the embodiment shown in FIG. 14, a reference voltage 158 generated bythe processor in the activator device provides a bias voltage to both ofthe bias rings 118. The bias voltage to the bias ring 118 surroundingthe first contact pad 108 is created by a first voltage divider 160while the bias voltage supplied to the bias ring 118 surrounding thesecond contact pad 110 is generated by a second voltage divider 162. Inthe embodiment illustrated, both the first voltage divider 160 and thesecond voltage divider 162 are formed from separate resistive networksthat include a series of resistors that divide the voltage referencesignal 158 to create a bias voltage of approximately 1.5 volts. Althoughthe voltage dividers 160, 162 are identical in the embodimentillustrated, it is contemplated that the voltage dividers could varydepending upon the specific requirements of the system. It is alsocontemplated the two voltage dividers 160, 162 could be connected to twoseparate control pins. In this manner, the voltage on each of the twoseparate control pins could be controlled separately such that the biasvoltage on the two bias rings could be controlled separately.Additionally, instead of using voltage dividers, any other means ofgenerating either a fixed or variable bias voltage level could be usedas long as the impedance level at the bias ring is high enough to allowfor sensing a voltage change due to leakage current and be safe in theoperating environment. Additionally or alternatively, instead of sensinga voltage change due to leakage current, current sensing could also beused while operating within the scope of the present disclosure.

If a fault exists in a way that there is conductive matter touching atleast one of the contact pads in a way that there is a risk of leakagecurrent flowing out of or into the contact pad, any leakage current thatexists will be detected at either one or both of the bias rings 118.These faults are most typically created when the contact surfaces getwet, either during use because of the patient sweating and the sealingis not tight or the contacts remain wet after cleaning and insufficientdrying. This type of fault can lead to leakage current going fromcontact pad to contact pad or through the patient. Additionally, debris,hair, worn out parts could also cause such a fault, which would resultin leakage current going from contact pad to contact pad.

Since both bias rings 118 are connected to the current leakage pins 152,154, the voltage on these two bias rings 118 will be sensed and theprocessor 26 of the activator module 3 can either generate an alarm orinterrupt the supply of power to the sensor device. Additionally oralternatively, the sensing circuit may be independent and separate fromthe processor 26 and operate to cut off connection to the power supplyin such an error condition. It is also possible to alter the biasvoltage of at least one bias ring during operation to furtherdifferentiate between various possible leakage routes (contact pad tocontact pad, contact pad(s) to an external return path in an ECGelectrode set, etc.). In such an embodiment, the reference voltage ateach of the bias rings must be able to be adjusted separately, asdescribed above.

Since the sensor device 2 and activator module 3 are designed to beconnected and disconnected on a regular basis, the sealing arrangementand voltage detection provide two separate forms of protection againstunacceptable amounts of leakage current that may be transferred to thepatient. Since the monitoring circuit of FIG. 14 continuously monitorsthe bias voltage on the pair of bias rings, any leakage current detectedat the interface between the contacts of the sensor device and theactivator can be detected with the activator module.

Referring back to FIG. 1, the sensor device 2 includes an identificationdevice 13 while the activator module 3 includes an ID receiver 18. It iscontemplated that the activator module 3 can be designed including anactuation switch 164 that can be depressed by a user when the sensordevice 2 is mated with the activator module 3. Upon depression of theswitch 164, a handshake process begins between the sensor device 2 andthe activator module 3. It is contemplated that the handshake willinvolve current levels under 100 μAmps and have a short duration toagain protect against any unwanted current transmission to the patient.Instead of using a switch, any other mechanism indicating the possiblemechanical connection of a sensor can be used, such as opticaldetectors, magnetic detectors or motion detectors.

This written description uses examples to disclose the invention,including the best mode, and also to enable any person skilled in theart to make and use the invention. The patentable scope of the inventionis defined by the claims, and may include other examples that occur tothose skilled in the art. Such other examples are intended to be withinthe scope of the claims if they have structural elements that do notdiffer from the literal language of the claims, or if they includeequivalent structural elements with insubstantial differences from theliteral languages of the claims.

We claim:
 1. A two part patient monitoring device, comprising: anactivator module including at least one power contact pad, a firstnon-galvanic data port and an internal battery; and a sensor device thatphysically connects to the activator module to create the patientmonitoring device, wherein the sensor device includes a sensor, at leastone power contact pin that engages the at least one power contact pad, asecond non-galvanic data port that communicates with the first data portand seal member that surrounds the power contact pad and the powercontact pin when the sensor device is connected to the activator module.2. The patient monitoring device of claim 1 wherein the activator moduleinclude two power contact pads and the sensor device includes two powercontact pins, wherein one of the seal members surrounds each of thepower contact pins.
 3. The patient monitoring device of claim 2 whereinthe two power contact pads are mounted to a contact surface, wherein theseal members engage the contact surface.
 4. The patient monitoringdevice of claim 1 wherein the activator module further comprises a biasring at least partially surrounding the power contact pad, wherein abias voltage is applied to the bias ring.
 5. The patient monitoringdevice of claim 4 wherein the activator module monitors the bias voltageapplied to the bias ring.
 6. The patient monitoring device of claim 4wherein the activator module includes a circuit that monitors the biasvoltage applied to the bias ring.
 7. The patient monitoring device 5wherein the activator module includes a processor that controls the biasvoltage applied to the bias ring.
 8. The patient monitoring device ofclaim 1 wherein the first and second non-galvanic data ports are opticaldata ports.
 9. The two part patient monitoring device of claim 5 whereinthe processor of the activator module automatically detects the type ofthe sensor device, such as a pulse oximeter sensor device, a temperaturesensor device, a blood pressure sensor device, a electrocardiograph(ECG) sensor device, or a electroencephalograph (EEG) sensor device; andwherein the activator module further comprises a display thatautomatically displays a connected device indicator to indicated whetherthe generic activator device is paired with the pulse oximeter sensordevice, the temperature sensor device, the blood pressure sensor device,the ECG sensor device, or the EEG sensor device.
 10. A two part patientmonitoring device, comprising: an activator module including at leastone power contact pad, a first non-galvanic data port, a bias ring atleast partially surrounding the power contact pad and an internalbattery; and a sensor device that physically connects to the activatormodule to create the patient monitoring device, wherein the sensordevice includes a sensor, at least one power contact pin that engagesthe at least one power contact pad and a second non-galvanic data portthat communicates with the first data port, wherein a bias voltage isapplied to the bias ring and the activator module monitors the biasvoltage applied to the bias ring.
 11. The patient monitoring device ofclaim 10 wherein the activator module includes a circuit that monitorsthe bias voltage applied to the bias ring.
 12. The patient monitoringdevice of claim 10 wherein the activator module includes a processorthat controls the bias voltage applied to the bias ring.
 13. The patientmonitoring device of claim 10 wherein the activator module include twopower contact pads and the sensor device includes two power contactpins, wherein one of the bias rings at least partially surrounds each ofthe power contact pads.
 14. The patient monitoring device of claim 12wherein the processor monitors for a change in the bias voltage oneither of the bias rings.
 15. The two part patient monitoring device ofclaim 10 wherein the processor of the activator module automaticallydetects the type of the sensor device, such as a pulse oximeter sensordevice, a temperature sensor device, a blood pressure sensor device, aelectrocardiograph (ECG) sensor device, or a electroencephalograph (EEG)sensor device; and wherein the activator module further comprises adisplay that automatically displays a connected device indicator toindicated whether the generic activator device is paired with the pulseoximeter sensor device, the temperature sensor device, the bloodpressure sensor device, the ECG sensor device, or the EEG sensor device.16. A two part patient monitoring device, comprising: an activatormodule including at least two power contact pads, a first non-galvanicdata port, a bias ring at least partially surrounding each of the powercontact pads, a processor and an internal battery; and a sensor devicethat physically connects to the activator module to create the patientmonitoring device, wherein the sensor device includes a sensor, at leasttwo power contact pins that each engage one of the power contact pads, asecond non-galvanic data port that communicates with the first data portand seal member that surrounds each of the power contact pads and thepower contact pins when the sensor device is connected to the activatormodule, wherein a bias voltage is applied to each of the bias rings andthe processor monitors the bias voltage applied to the bias rings. 17.The patient monitoring device of claim 16 wherein the two power contactpads are mounted to a contact surface, wherein the seal members eachengage the contact surface.
 18. The two part patient monitoring deviceof claim 16 wherein the processor of the activator module automaticallydetects the type of the sensor device, such as a pulse oximeter sensordevice, a temperature sensor device, a blood pressure sensor device, aelectrocardiograph (ECG) sensor device, or a electroencephalograph (EEG)sensor device; and wherein the activator module further comprises adisplay that automatically displays a connected device indicator toindicated whether the generic activator device is paired with the pulseoximeter sensor device, the temperature sensor device, the bloodpressure sensor device, the ECG sensor device, or the EEG sensor device.19. The two part patient monitoring device of claim 16 furthercomprising a first identification device in the activator module and asecond identification device in the sensor device, wherein the first andsecond identification devices communication with each other when theactivator module is connected to the sensor device.
 20. The two partpatient monitoring device of claim 16 wherein the activator module isreceivable in the sensor device or another sensor device.